| Literature DB >> 26289821 |
María D Segarra-Maset1, Beatriu Escuder2, Juan F Miravet3.
Abstract
A molecular hydrogel formed by a derivative of L-valine with pendant isonicotinoyl moieties interacts selectively with protonated dopamine in the presence of related compounds such as 3-methylcatechol, and protonated or neutral phenethylamine. A two-point interaction with the gel fibers is postulated to explain the results. The conclusions are obtained from nuclear magnetic resonance saturation transfer experiments (STD-NMR), illustrating how this technique is perfectly suited to monitor the interaction of substrates with the fibrillar network of a molecular gel.Entities:
Keywords: NMR spectroscopy; hydrogels; molecular recognition; soft materials; supramolecular chemistry
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Year: 2015 PMID: 26289821 DOI: 10.1002/chem.201502018
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236